The F1F0 ATP synthase and mitochondrial respiratory chain complexes are present on the plasma membrane of an osteosarcoma cell line: An immunocytochemical study

Mitochondrion ◽  
2006 ◽  
Vol 6 (6) ◽  
pp. 305-314 ◽  
Author(s):  
Sarah K. Yonally ◽  
Roderick A. Capaldi
Keyword(s):  
Plasma Membrane ◽  
Cell Line ◽  
Respiratory Chain ◽  
Atp Synthase ◽  
Mitochondrial Respiratory Chain ◽  
Osteosarcoma Cell ◽  
Immunocytochemical Study ◽  
Respiratory Chain Complexes ◽  
Chain Complexes ◽  
F1f0 Atp Synthase

scholarly journals Effect of inhibitors of mitochondrial respiratory chain complexes on the electromechanical activity in human myocardium

Medicina ◽  
2010 ◽  
Vol 46 (10) ◽  
pp. 679
Author(s):  
Vida Gendvilienė ◽  
Irma Martišienė ◽  
Danguolė Zablockaitė ◽  
Jonas Jurevičius
Keyword(s):  
Respiratory Chain ◽  
Control Level ◽  
Chain Complex ◽  
Mitochondrial Respiratory Chain ◽  
Human Myocardium ◽  
Contraction Force ◽  
Respiratory Chain Complexes ◽  
Complex Iv ◽  
Resting Tension ◽  
Chain Complexes

The aim of the study was to investigate the effect of inhibitors of mitochondrial respiratory chain complexes I, III, and IV on the electromechanical activity in human myocardium. Material and methods. The experiments were performed on the human myocardial strips obtained from patients with heart failure (NYHA class III or IV) using a conventional method of registration of myocardial electromechanical activity. Under the perfusion with physiological Tyrode solution (control), contraction force (P) was 0.94±0.12 mN (n=16), relaxation time (t50) was 173.38±5.03 ms (n=15), action potential durations measured at 50% (AP50) and 90% (AP90) repolarization were 248.96±13.38 ms and 398.59±17.93 ms, respectively (n=13). Results. The inhibition of respiratory chain complex I by rotenone (3×10–5 M, the highest concentration applied) decreased contraction force of human myocardium to 48.99%±14.74% (n=3) (P<0.05); AP50, to 81.34%±15.81%; and AP90, to 87.28%±7.25% (n=3) (P>0.05) of control level, while relaxation time and resting tension remained almost unchanged. Antimycin A, an inhibitor of complex III, applied at the highest concentration (3×10–4 M) reduced P to 41.66%±8.8% (n=5) (P<0.001) and marginally increased t50 and decreased the durations of AP. Anoxia (3 mM Na2S2O4) that inhibits the activity of complex IV reduced the contraction force to 9.23%±3.56% (n=6) (P<0.001), AP50 and AP90 to 65.46%±9.95% and 71.07%±8.39% (n=5) (P<0.05) of control level, respectively; furthermore, the resting tension augmented (contracture developed). Conclusions. Our results show that the inhibition of respiratory chain complex IV had the strongest inhibitory effect on the electromechanical activity of failing human myocardium.

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